| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017953-61018180 | Common:2; Rare:87 | ||||
| chr2:61018150-61018550 | Common:3; Rare:276 | ||||
| chr2:61065614-61066014 | Common:9; Rare:377 | ||||
| chr2:61066133-61066533 | Common:2; Rare:235 | ||||
| chr2:61066446-61066846 | Common:3; Rare:156 | ||||
| chr2:61176763-61177640 | Common:43; Rare:1193 | ||||
| chr2:61177662-61178279 | Common:10; Rare:312 | ||||
| chr2:61470007-61470237 | Common:3; Rare:58 | ||||
| chr2:61470610-61471492 | Common:29; Rare:1551 | ||||
| chr2:61536352-61537320 | Common:19; Rare:1026 | ||||
| chr2:61537236-61538160 | Common:22; Rare:822 | ||||
| chr2:61538120-61538633 | Common:6; Rare:356 | ||||
| chr2:61538570-61539080 | Common:6; Rare:747 | ||||
| chr2:61853630-61854327 | Common:13; Rare:643; Clinvar:7; Clinvar (benign):6 | ||||
| chr2:61854410-61854760 | Common:1; Rare:148 |